- a method to identify potential exon/intron structure in pre-mRNA by splice site prediction and spliced alignment
Species (selects species-specific splice site model) human mouse rat chicken Drosophila Daphnia nematode yeast Aspergillus Arabidopsis maize rice Medicago generic
Sequences should be in the one-letter-code ({a,b,c,g,h,k,m,n,r,s,t,u,w,y}), upper or lower case; all other characters are ignored during input. Multiple sequence input is accepted in FASTA format (sequences separated by identifier lines of the form >SQ;name_of_sequence comments) or in GenBank format.
Paste your genomic DNA sequence here:... or upload your sequence file (specify file name):... or type in the GenBank accession number of your sequence:Select format: plain FASTA GenBank Sequence name: (optional, used in plain sequence format only) From position: to position: Strand: original reverse both
Spliced Alignment: The output will show an optimal threading of a significantly matching cDNA/EST sequence into the genomic DNA by aligning putative exons only and displaying putative introns as (long) gaps in the cDNA/EST.
Select pre-processed EST database NOT SET Drosophila C.elegans Plant OR paste your own cDNA/EST sequence(s) here ( FASTA format ):... and/or upload your cDNA/EST sequence file (specify file name):
Select "alignment stringency level" allowed user to select parameter to GeneSeqerWS. "Strict" invokes "-x 30 -y 45 -z 60", moderate "-x 16 -y 24 -z 48", and low "-x 12 -y 12 -z 30" argument to GeneSeqerWS.
Select alignment stringency level: strict moderate low
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